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성함이나 학술지명, PMID로 찾아보십시오.
Rust C에 대해
49건, 그중 20건 표시.
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
외 70명 — 모두 보기
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
페이지 4개
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Eyre S,
Bowes J,
Diogo D,
Lee A,
Barton A,
Martin P,
Zhernakova A,
Stahl E,
Viatte S,
McAllister K,
Amos CI,
Padyukov L
외 32명 — 모두 보기
Toes RE,
Huizinga TW,
Wijmenga C,
Trynka G,
Franke L,
Westra HJ,
Alfredsson L,
Hu X,
Sandor C,
de Bakker PI,
Davila S,
Khor CC,
Heng KK,
Andrews R,
Edkins S,
Hunt SE,
Langford C,
Symmons D,
Concannon P,
Onengut-Gumuscu S,
Rich SS,
Deloukas P,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Ärlsetig L,
Martin J,
Rantapää-Dahlqvist S,
Plenge RM,
Raychaudhuri S,
Klareskog L,
Gregersen PK,
Worthington J
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
페이지 4개
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
Cortes A,
Hadler J,
Pointon JP,
Robinson PC,
Karaderi T,
Leo P,
Cremin K,
Pryce K,
Harris J,
Lee S,
Joo KB,
Shim SC
외 53명 — 모두 보기
Weisman M,
Ward M,
Zhou X,
Garchon HJ,
Chiocchia G,
Nossent J,
Lie BA,
Førre Ø,
Tuomilehto J,
Laiho K,
Jiang L,
Liu Y,
Wu X,
Bradbury LA,
Elewaut D,
Burgos-Vargas R,
Stebbings S,
Appleton L,
Farrah C,
Lau J,
Kenna TJ,
Haroon N,
Ferreira MA,
Yang J,
Mulero J,
Fernandez-Sueiro JL,
Gonzalez-Gay MA,
Lopez-Larrea C,
Deloukas P,
Donnelly P,
Bowness P,
Gafney K,
Gaston H,
Gladman DD,
Rahman P,
Maksymowych WP,
Xu H,
Crusius JB,
van der Horst-Bruinsma IE,
Chou CT,
Valle-Oñate R,
Romero-Sánchez C,
Hansen IM,
Pimentel-Santos FM,
Inman RD,
Videm V,
Martin J,
Breban M,
Reveille JD,
Evans DM,
Kim TH,
Wordsworth BP,
Brown MA
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) 외 컨소시엄 4곳
Nature genetics · 2013 · PMID 23749187
페이지 4개
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Hysi PG,
Cheng CY,
Springelkamp H,
Macgregor S,
Bailey JNC,
Wojciechowski R,
Vitart V,
Nag A,
Hewitt AW,
Höhn R,
Venturini C,
Mirshahi A
외 79명 — 모두 보기
Ramdas WD,
Thorleifsson G,
Vithana E,
Khor CC,
Stefansson AB,
Liao J,
Haines JL,
Amin N,
Wang YX,
Wild PS,
Ozel AB,
Li JZ,
Fleck BW,
Zeller T,
Staffieri SE,
Teo YY,
Cuellar-Partida G,
Luo X,
Allingham RR,
Richards JE,
Senft A,
Karssen LC,
Zheng Y,
Bellenguez C,
Xu L,
Iglesias AI,
Wilson JF,
Kang JH,
van Leeuwen EM,
Jonsson V,
Thorsteinsdottir U,
Despriet DDG,
Ennis S,
Moroi SE,
Martin NG,
Jansonius NM,
Yazar S,
Tai ES,
Amouyel P,
Kirwan J,
van Koolwijk LME,
Hauser MA,
Jonasson F,
Leo P,
Loomis SJ,
Fogarty R,
Rivadeneira F,
Kearns L,
Lackner KJ,
de Jong PTVM,
Simpson CL,
Pennell CE,
Oostra BA,
Uitterlinden AG,
Saw SM,
Lotery AJ,
Bailey-Wilson JE,
Hofman A,
Vingerling JR,
Maubaret C,
Pfeiffer N,
Wolfs RCW,
Lemij HG,
Young TL,
Pasquale LR,
Delcourt C,
Spector TD,
Klaver CCW,
Small KS,
Burdon KP,
Stefansson K,
Wong TY,
Viswanathan A,
Mackey DA,
Craig JE,
Wiggs JL,
van Duijn CM,
Hammond CJ,
Aung T
BMES GWAS Group · NEIGHBORHOOD Consortium 외 컨소시엄 1곳
Nature genetics · 2014 · PMID 25173106 · open access
페이지 4개
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Zeggini E,
Weedon MN,
Lindgren CM,
Frayling TM,
Elliott KS,
Lango H,
Timpson NJ,
Perry JR,
Rayner NW,
Freathy RM,
Barrett JC,
Shields B
외 14명 — 모두 보기
Morris AP,
Ellard S,
Groves CJ,
Harries LW,
Marchini JL,
Owen KR,
Knight B,
Cardon LR,
Walker M,
Hitman GA,
Morris AD,
Doney AS,
McCarthy MI,
Hattersley AT
Wellcome Trust Case Control Consortium (WTCCC)
Science (New York, N.Y.) · 2007 · PMID 17463249
페이지 3개
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
Todd JA,
Walker NM,
Cooper JD,
Smyth DJ,
Downes K,
Plagnol V,
Bailey R,
Nejentsev S,
Field SF,
Payne F,
Lowe CE,
Szeszko JS
외 28명 — 모두 보기
Hafler JP,
Zeitels L,
Yang JH,
Vella A,
Nutland S,
Stevens HE,
Schuilenburg H,
Coleman G,
Maisuria M,
Meadows W,
Smink LJ,
Healy B,
Burren OS,
Lam AA,
Ovington NR,
Allen J,
Adlem E,
Leung HT,
Wallace C,
Howson JM,
Guja C,
Ionescu-Tîrgovişte C,
Simmonds MJ,
Heward JM,
Gough SC,
Dunger DB,
Wicker LS,
Clayton DG
Genetics of Type 1 Diabetes in Finland · Wellcome Trust Case Control Consortium
Nature genetics · 2007 · PMID 17554260
페이지 3개
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Lindgren CM,
Heid IM,
Randall JC,
Lamina C,
Steinthorsdottir V,
Qi L,
Speliotes EK,
Thorleifsson G,
Willer CJ,
Herrera BM,
Jackson AU,
Lim N
외 131명 — 모두 보기
Scheet P,
Soranzo N,
Amin N,
Aulchenko YS,
Chambers JC,
Drong A,
Luan J,
Lyon HN,
Rivadeneira F,
Sanna S,
Timpson NJ,
Zillikens MC,
Zhao JH,
Almgren P,
Bandinelli S,
Bennett AJ,
Bergman RN,
Bonnycastle LL,
Bumpstead SJ,
Chanock SJ,
Cherkas L,
Chines P,
Coin L,
Cooper C,
Crawford G,
Doering A,
Dominiczak A,
Doney AS,
Ebrahim S,
Elliott P,
Erdos MR,
Estrada K,
Ferrucci L,
Fischer G,
Forouhi NG,
Gieger C,
Grallert H,
Groves CJ,
Grundy S,
Guiducci C,
Hadley D,
Hamsten A,
Havulinna AS,
Hofman A,
Holle R,
Holloway JW,
Illig T,
Isomaa B,
Jacobs LC,
Jameson K,
Jousilahti P,
Karpe F,
Kuusisto J,
Laitinen J,
Lathrop GM,
Lawlor DA,
Mangino M,
McArdle WL,
Meitinger T,
Morken MA,
Morris AP,
Munroe P,
Narisu N,
Nordström A,
Nordström P,
Oostra BA,
Palmer CN,
Payne F,
Peden JF,
Prokopenko I,
Renström F,
Ruokonen A,
Salomaa V,
Sandhu MS,
Scott LJ,
Scuteri A,
Silander K,
Song K,
Yuan X,
Stringham HM,
Swift AJ,
Tuomi T,
Uda M,
Vollenweider P,
Waeber G,
Wallace C,
Walters GB,
Weedon MN,
Witteman JC,
Zhang C,
Zhang W,
Caulfield MJ,
Collins FS,
Davey Smith G,
Day IN,
Franks PW,
Hattersley AT,
Hu FB,
Jarvelin MR,
Kong A,
Kooner JS,
Laakso M,
Lakatta E,
Mooser V,
Morris AD,
Peltonen L,
Samani NJ,
Spector TD,
Strachan DP,
Tanaka T,
Tuomilehto J,
Uitterlinden AG,
van Duijn CM,
Wareham NJ,
Hugh Watkins,
Waterworth DM,
Boehnke M,
Deloukas P,
Groop L,
Hunter DJ,
Thorsteinsdottir U,
Schlessinger D,
Wichmann HE,
Frayling TM,
Abecasis GR,
Hirschhorn JN,
Loos RJ,
Stefansson K,
Mohlke KL,
Barroso I,
McCarthy MI
Wellcome Trust Case Control Consortium · Procardis Consortia 외 컨소시엄 1곳
PLoS genetics · 2009 · PMID 19557161 · open access
페이지 3개
Genome-wide association study identifies five loci associated with lung function
Repapi E,
Sayers I,
Wain LV,
Burton PR,
Johnson T,
Obeidat M,
Zhao JH,
Ramasamy A,
Zhai G,
Vitart V,
Huffman JE,
Igl W
외 83명 — 모두 보기
Albrecht E,
Deloukas P,
Henderson J,
Granell R,
McArdle WL,
Rudnicka AR,
Barroso I,
Loos RJ,
Wareham NJ,
Mustelin L,
Rantanen T,
Surakka I,
Imboden M,
Wichmann HE,
Grkovic I,
Jankovic S,
Zgaga L,
Hartikainen AL,
Peltonen L,
Gyllensten U,
Johansson A,
Zaboli G,
Campbell H,
Wild SH,
Wilson JF,
Gläser S,
Homuth G,
Völzke H,
Mangino M,
Soranzo N,
Spector TD,
Polasek O,
Rudan I,
Wright AF,
Heliövaara M,
Ripatti S,
Pouta A,
Naluai AT,
Olin AC,
Torén K,
Cooper MN,
James AL,
James AL,
Palmer LJ,
Hingorani AD,
Wannamethee SG,
Whincup PH,
Smith GD,
Ebrahim S,
McKeever TM,
Pavord ID,
MacLeod AK,
Morris AD,
Porteous DJ,
Cooper C,
Dennison E,
Shaheen S,
Karrasch S,
Schnabel E,
Schulz H,
Grallert H,
Bouatia-Naji N,
Delplanque J,
Froguel P,
Blakey JD,
Britton JR,
Morris RW,
Holloway JW,
Lawlor DA,
Hui J,
Nyberg F,
Jarvelin MR,
Jackson C,
Kähönen M,
Kaprio J,
Probst-Hensch NM,
Koch B,
Hayward C,
Evans DM,
Elliott P,
Strachan DP,
Hall IP,
Tobin MD
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
페이지 3개
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Waterworth DM,
Ricketts SL,
Song K,
Chen L,
Zhao JH,
Ripatti S,
Aulchenko YS,
Zhang W,
Yuan X,
Lim N,
Luan J,
Ashford S
외 54명 — 모두 보기
Wheeler E,
Young EH,
Hadley D,
Thompson JR,
Braund PS,
Johnson T,
Struchalin M,
Surakka I,
Luben R,
Khaw KT,
Rodwell SA,
Loos RJ,
Boekholdt SM,
Inouye M,
Deloukas P,
Elliott P,
Schlessinger D,
Sanna S,
Scuteri A,
Jackson A,
Mohlke KL,
Tuomilehto J,
Roberts R,
Stewart A,
Kesäniemi YA,
Mahley RW,
Grundy SM,
McArdle W,
Cardon L,
Waeber G,
Vollenweider P,
Chambers JC,
Boehnke M,
Abecasis GR,
Salomaa V,
Järvelin MR,
Ruokonen A,
Barroso I,
Epstein SE,
Hakonarson HH,
Rader DJ,
Reilly MP,
Witteman JC,
Hall AS,
Samani NJ,
Strachan DP,
Barter P,
van Duijn CM,
Kooner JS,
Peltonen L,
Wareham NJ,
McPherson R,
Mooser V,
Sandhu MS
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
페이지 3개
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
외 81명 — 모두 보기
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21743469
페이지 3개
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani P,
Burdon KP,
Fogarty R,
Sharma S,
Hewitt AW,
Martin S,
Law MH,
Cremin K,
Bailey JNC,
Loomis SJ,
Pasquale LR,
Haines JL
외 30명 — 모두 보기
Hauser MA,
Viswanathan AC,
McGuffin P,
Topouzis F,
Foster PJ,
Graham SL,
Casson RJ,
Chehade M,
White AJ,
Zhou T,
Souzeau E,
Landers J,
Fitzgerald JT,
Klebe S,
Ruddle JB,
Goldberg I,
Healey PR,
Mills RA,
Wang JJ,
Montgomery GW,
Martin NG,
RadfordSmith G,
Whiteman DC,
Brown MA,
Brown MA,
Wiggs JL,
Mackey DA,
Mitchell P,
MacGregor S,
Craig JE
Wellcome Trust Case Control Consortium 2, NEIGHBORHOOD consortium
Nature genetics · 2014 · PMID 25173105 · open access
페이지 3개
Common variants near TERC are associated with mean telomere length
Codd V,
Mangino M,
van der Harst P,
Braund PS,
Kaiser M,
Beveridge AJ,
Rafelt S,
Moore J,
Nelson C,
Soranzo N,
Zhai G,
Valdes AM
외 16명 — 모두 보기
Blackburn H,
Mateo Leach I,
de Boer RA,
Kimura M,
Aviv A,
Goodall AH,
Ouwehand W,
van Veldhuisen DJ,
van Gilst WH,
Navis G,
Burton PR,
Tobin MD,
Hall AS,
Thompson JR,
Spector T,
Samani NJ
Wellcome Trust Case Control Consortium
Nature genetics · 2010 · PMID 20139977
페이지 2개
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
Zhou K,
Bellenguez C,
Spencer CC,
Bennett AJ,
Coleman RL,
Tavendale R,
Hawley SA,
Donnelly LA,
Schofield C,
Groves CJ,
Burch L,
Carr F
외 38명 — 모두 보기
Strange A,
Freeman C,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Gray E,
Hunt S,
Jankowski J,
Langford C,
Markus HS,
Mathew CG,
Plomin R,
Rautanen A,
Sawcer SJ,
Samani NJ,
Trembath R,
Viswanathan AC,
Wood NW,
Harries LW,
Hattersley AT,
Doney AS,
Colhoun H,
Morris AD,
Sutherland C,
Hardie DG,
Peltonen L,
McCarthy MI,
Holman RR,
Palmer CN,
Donnelly P,
Pearson ER
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group · Wellcome Trust Case Control Consortium 2 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21186350 · open access
페이지 2개
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies
Reilly MP,
Li M,
He J,
Ferguson JF,
Stylianou IM,
Mehta NN,
Burnett MS,
Devaney JM,
Knouff CW,
Thompson JR,
Horne BD,
Stewart AF
외 20명 — 모두 보기
Assimes TL,
Wild PS,
Allayee H,
Nitschke PL,
Patel RS,
Martinelli N,
Girelli D,
Quyyumi AA,
Anderson JL,
Erdmann J,
Hall AS,
Schunkert H,
Quertermous T,
Blankenberg S,
Hazen SL,
Roberts R,
Kathiresan S,
Samani NJ,
Epstein SE,
Rader DJ
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Lancet (London, England) · 2011 · PMID 21239051
페이지 2개
Seven newly identified loci for autoimmune thyroid disease
Cooper JD,
Simmonds MJ,
Walker NM,
Burren O,
Brand OJ,
Guo H,
Wallace C,
Stevens H,
Coleman G,
Franklyn JA,
Todd JA,
Gough SC
Wellcome Trust Case Control Consortium
Human molecular genetics · 2012 · PMID 22922229 · open access
페이지 2개
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
외 96명 — 모두 보기
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
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